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SLC26A7

Gene

solute carrier family 26 member 7

HGNCHGNC:14467EnsemblENSG00000147606NCBI Gene115111
Locus: gene with protein productLocation: 8q21.3

Also known as

Symbols and names change; identity (the HGNC ID) does not. Previous and alternative forms are kept distinct.

Also known asSUT2
View full nomenclature history (5)
Alias symbolsSUT2
Previous namessolute carrier family 26, member 7, solute carrier family 26 (anion exchanger), member 7
Alias namesAnion exchange transporter, sulfate anion transporter 2

Associated diseases

via associated_with

Diseases linked to this gene through the canonical GENE→DISEASE (associated_with) relation, drawn from Open Targets' top-ranked associations by overall score — not the full association set. Disease-level detail lives on each disease's own page.

Congenital Hypothyroidism
Smoking initiation
Actinic keratosis
Genetic Diseases, Inborn
Bipolar Disorder
Alopecia

Drawn from Open Targets’ top 10 associations by overall score for this gene — the subset resolved to a canonical disease. Lower-ranked associations, and diseases not yet canonicalised, are not shown.

Gene family

HGNC gene-group membership.

Solute carrier family 26

Provenance

HGNCCanonical human gene identity from HGNC (release 2026-07-07), updated 2023-01-20.
Open TargetsGene–disease associations from the Open Targets Platform.